Abstract
Synthetic coat protein complex I (COPI)-coated vesicles form spontaneously from large ( approximately 300 nm in diameter), chemically defined liposomes incubated with coatomer, Arf1p, and guanosine 5'-[gamma-thio]triphosphate. Coated vesicles are 40-70 nm in diameter, approximately the size of COPI vesicles formed from native membranes. The formation of COPI-coated buds and vesicles and the binding of Arf1p to donor liposomes depends on guanosine 5'-[gamma-thio]triphosphate. In contrast to the behavior of the COPII coat, coatomer binds to liposomes containing a variety of charged or neutral phospholipids. However, the formation of COPI buds and vesicles is stimulated by acidic phospholipids. In the absence of Arf1p, coatomer binds to liposomes containing dioleoylphosphatidic acid as a sole acidic phospholipid to form large coated surfaces without forming COPI-coated buds or vesicles. We conclude that Arf1p-GTP and coatomer comprise the minimum apparatus necessary to create a COPI-coated vesicle.
MeSH Terms
ADP-Ribosylation Factor 1
ADP-Ribosylation Factors
Centrifugation, Density Gradient
Coated Vesicles/metabolism,ultrastructure
Coatomer Protein
GTP-Binding Proteins/physiology
Guanosine Triphosphate/physiology
Lipid Metabolism
Liposomes/metabolism
Membrane Proteins/metabolism,physiology
Microscopy, Electron
Particle Size
Phospholipase D/physiology
Phospholipids/chemistry
Chemicals
Coatomer Protein
Liposomes
Membrane Proteins
Phospholipids
Guanosine Triphosphate
Phospholipase D
GTP-Binding Proteins
ADP-Ribosylation Factor 1
ADP-Ribosylation Factors
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Spang A
Department of Molecular and Cell Biology and Howard Hughes Medical Institute, University of California, Berkeley, CA 94720, USA.
Matsuoka K
Hamamoto S
Schekman R
Orci L
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